National CADDRE Study: Child
Development and Autism
<date>
Dear Mr./Ms. <name>:
Thank you for taking part in the National CADDRE Study: Child Development and Autism. An important part of this study is to collect information from medical records.
Collecting information from medical records will help us to learn about medical events and history that may be important to child development. Medical records often contain important information that is difficult to remember, such as fevers or illnesses, prescribed medications, and exact dates. For this reason, we would like to look at the medical records of the biological mother from all medical providers seen during the three years prior to <child’s name> date of birth. We would also like to look at the birth hospital record and pediatric records of your child. It is very important for us to look at the records of all types of families, even if the family does not have a child who has a developmental delay. Learning more about the differences in children’s medical records may give us clues about child development.
We must have your written consent in order to collect information from medical records. By signing the enclosed Health Insurance Portability and Accountability Act (HIPAA) forms for each provider, you give us permission to collect information from the medical records. Further, we ask that you please mark off the type of provider for which you have given us permission to contact on the check list in the enclosed packet.
It is important for us to look at records of biological mothers. If you are not the biological mother of your child, we ask that you please provide us with her contact information. You can write this information on the form instead of signing.
Please return the signed HIPAA forms and provider checklist in the envelope provided. You can also give the forms to study staff at your first study visit. If you have any questions about the study or the enclosed forms, you can call < study coordinator contact info>.
Thank you again for taking part in this important study.
Sincerely,
<Project Coordinator>
Provider Check List
Please check the box of all the providers for which you have given us permission to contact to access the biological mother’s and child’s medical records. We are asking you to complete this checklist to ensure that we have the ability to collect as complete medical information as possible on the biological mother and child.
Biological Mother:
□ Primary Care Physician (example: family doctor or internal medicine)
□ Obstetrician
□ Gynecologist
□ Allergist/Immunologist
□ Rheumatologist
□ Psychiatrist
□ Infertility specialist/reproductive endocrinologist
□ Other (Please specify): _____________________________
Child in study:
□ Pediatrician
□ Developmental Pediatrician
□ Allergist/Immunologist
□ Psychiatrist
□ Neurologist
□ Other (Please specify): _______________________________
Health Information Portability and Accountability Act (HIPAA) Medical Records Release Authorization Form
Patient Name: |
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Phone: |
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Street Address: |
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Date of Birth |
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SS # (last 4 digits) |
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<< site specific information>> |
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The information identified below may be used by or disclosed to the following individuals/organizations: |
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Name: << site specific information>> |
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Address: << site specific information>>
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Medical Provider (name & address):
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Please specify the parts and dates to be released below. |
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Dates of Service: |
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Types of Information (Check all that apply below. It is NOT necessary to check the boxes below, unless you disagree with statement #3 above): |
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Gynecology & Obstetric Records Labor and Delivery Record Pediatric Record Anthropometric (growth) measurements Consultation Reports Discharge Summary/Instructions ER (emergency room) records |
Face Sheets/Registration Sheets HIV Information Hospital Admissions Information Injection/Vaccination Information Lab Results Medication List Medical History Mental Health Information |
Pathology Report Post-Operative Reports Procedural Information Progress Notes Radiology (Ultrasound) Reports Referral Sheets Substance Abuse Information Surgical History ___________________ |
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5. The information that I am authorizing this disclosure will be solely used for the purpose of state what kind of __________________research. |
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6. I understand that I have a right to revoke this authorization at any time. If I choose to revoke this authorization, I must do so in writing, and submit my written request to the medical records department of this facility. I also understand that any information that the researchers collect before I choose to revoke this authorization will be retained by the researchers. |
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7. I understand that unless revoked, this authorization will expire at the end of the CADDRE case cohort research study. |
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8. I understand that because sensitive information is collected in this study, <<CDC>> received a <<‘Certificate of Confidentiality.’>> This means that any information that <<CDC>> has that identifies you or your child will be used only for this project. It cannot be given, used, or disclosed to anyone else unless you give your written consent (or unless required by law). |
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9. I understand that this disclosure is voluntary and my decision to authorize or not authorize the release of this information will not affect my ability to be treated at the above mentioned facilities. |
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Participant Signature |
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Date |
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If signed by legal representative, relationship to participant |
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Date |
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Signature of Witness |
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Date |
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Appendix E18
File Type | application/msword |
Author | Laura Davis |
Last Modified By | pax1 |
File Modified | 2006-12-29 |
File Created | 2006-12-29 |